L-Homoarginine Hydrochloride - ≥98% , CAS No.1483-01-8

CAS: 1483-01-8 Cat. No.: H100536 Peso molecular: 224.69 Beilstein Registry Number: 4016621 Número EC: 216-045-6 PubChem CID: 2723930
Disponible para pedir
GRADE & PURITY ≥98%
Synonyms
L-HOMOARGININE HCL | H-HomoArg-OH.HCl | C7H17ClN4O2 | N6-(Aminoiminomethyl)-L-lysine Hydrochloride | L-Homoarginine hydrochloride | H-HomoArg-OH | DTXSID201342617 | AS-12991 | AKOS015924239 | AMY14323 | H1172 | L(+)-Homoarginine hydrochloride | SCHEMBL710
Storage
Store at 2-8°C
Shipped In
Wet ice
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
1g
H100536-1g
1
9,90US$
5g
H100536-5g
3
25,90US$
25g
H100536-25g
3
99,90US$
100g
H100536-100g
2
359,90US$
Enter a quantity for the sizes you want to add.
🧪

Why this grade

≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at 2-8°C Ships Wet ice Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Sinónimos
L-HOMOARGININE HCL | H-HomoArg-OH.HCl | C7H17ClN4O2 | N6-(Aminoiminomethyl)-L-lysine Hydrochloride | L-Homoarginine hydrochloride | H-HomoArg-OH | DTXSID201342617 | AS-12991 | AKOS015924239 | AMY14323 | H1172 | L(+)-Homoarginine hydrochloride | SCHEMBL710
Especificaciones y pureza
≥98%
Mecanismos bioquímicos y fisiológicos
Homoarginine is an inhibitor of tissue-specific alkaline phosphatase (TNALP). It is also an inhibitor of arginine cell transport through sodium-independent high affinity y+transporter.
Condiciones de almacenamiento de almacenamiento
Store at 2-8°C
Enviado en
Wet ice
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Pureza
≥98%
Nombres e identificadores
Pubchem Sid488192222
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488192222
Sonrisas canónicasC(CCN=C(N)N)CC(C(=O)O)N.Cl
IUPAC Name(2S)-2-amino-6-(diaminomethylideneamino)hexanoic acid;hydrochloride
InChIKeyYMKBVNVCKUYUDM-JEDNCBNOSA-N
INCHI1S/C7H16N4O2.ClH/c8-5(6(12)13)3-1-2-4-11-7(9)10;/h5H,1-4,8H2,(H,12,13)(H4,9,10,11);1H/t5-;/m0./s1
Isómeros SMILES C(CCN=C(N)N)C[C@@H](C(=O)O)N.Cl
WGK Alemania 3
PubChem CID 2723930
Peso molecular 224.69
Beilstein 4016621
Reaxy-Rn 4016621

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganic acids and derivatives
ClaseCarboxylic acids and derivatives
SubclassAmino acids, peptides, and analogues
Intermediate Tree Nodes Amino acids and derivatives - Alpha amino acids and derivatives - Alpha amino acids
Direct ParentL-alpha-amino acids
Alternative Parents Medium-chain fatty acids  Guanidines  Amino acids  Propargyl-type 1,3-dipolar organic compounds  Monocarboxylic acids and derivatives  Carboxylic acids  Carboximidamides  Organopnictogen compounds  Organic oxides  Monoalkylamines  Hydrochlorides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAliphatic acyclic compounds
Substituents L-alpha-amino acid - Medium-chain fatty acid - Fatty acid - Fatty acyl - Guanidine - Amino acid - Carboxylic acid - Monocarboxylic acid or derivatives - Carboximidamide - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Carbonyl group - Organic oxygen compound - Primary amine - Organooxygen compound - Organonitrogen compound - Amine - Primary aliphatic amine - Organic nitrogen compound - Organopnictogen compound - Organic oxide - Hydrochloride - Hydrocarbon derivative - Aliphatic acyclic compound
DescripciónThis compound belongs to the class of organic compounds known as l-alpha-amino acids. These are alpha amino acids which have the L-configuration of the alpha-carbon atom.
External Descriptors Not available
Estructura 3D
Modelo de Estructura Química Interactiva





Certificados (CoA, COO, BSE/TSE y tabla de análisis)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

10 results found

Lot NumberCertificate TypeFechaArticulo
K21251015Certificate of AnalysisSep 08, 2025 H100536
F1912243Certificate of AnalysisApr 11, 2023 H100536
C2302688Certificate of AnalysisJan 17, 2023 H100536
C2302706Certificate of AnalysisJan 17, 2023 H100536
C2302707Certificate of AnalysisJan 17, 2023 H100536
C2302710Certificate of AnalysisJan 17, 2023 H100536
C2302719Certificate of AnalysisJan 17, 2023 H100536
E2619189Certificate of AnalysisJan 17, 2023 H100536
C2302705Certificate of AnalysisDec 19, 2022 H100536
C1517154Certificate of AnalysisNov 11, 2022 H100536
Propiedades químicas y físicas
SolubilidadSoluble in water(50 mg/mL).
SensibilidadMoisture sensitive
Rotación específica [α]18° (C=8.6N,HCl)
Punto de fusión (°C)213-215°C
Peso molecular224.690 g/mol
XLogP3
Hydrogen Bond Donor Count5
Hydrogen Bond Acceptor Count4
Rotatable Bond Count6
Exact Mass224.104 Da
Monoisotopic Mass224.104 Da
Topological Polar Surface Area128.000 Ų
Heavy Atom Count14
Formal Charge0
Complexity189.000
Isotope Atom Count0
Defined Atom Stereocenter Count1
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count2
Citations of This Product
Referencias
1. Chi Yan, Xingyu Chen, Wenqing Gao, Chunlan Tang, Liwen Du, Chengyi Xie, Feng Xu, Keqi Tang, Jiancheng Yu.  (2025)  Chiral Derivatization Enables High-Resolution Ion Mobility Spectrometry of 30 Amino Acid Enantiomers.  ANALYTICAL CHEMISTRY,      [PMID:41451537] [10.1021/acs.analchem.5c06382]
Calculadoras de soluciones
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